Evidence map›Paper›PMID 9858552›Full record

ArticleMolecular and cellular biology1999

Cux/CDP homeoprotein is a component of NF-muNR and represses the immunoglobulin heavy chain intronic enhancer by antagonizing the bright transcription activator.

Z Wang, A Goldstein, R T Zong, D Lin, E J Neufeld, R H Scheuermann, P W Tucker

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.3field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 80 citations in OpenAlex.

  1. The IgHFrontiers in immunology · 2023
    Article
  2. Review
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  7. Regulation of cell proliferation and differentiation in the kidney.Frontiers in bioscience (Landmark edition) · 2009
    Review
  8. Article
  9. Article
  10. Article
  11. CCAAT displacement protein/cut homolog recruits G9a histone lysine methyltransferase to repress transcription.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  12. Article
  13. Article
  14. Article
  15. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Z WangDepartment of Pathology and Laboratory of Molecular Pathology, The University of Texas Southwestern Medical Center, Dallas, Texas 75235-9072, USA.
A Goldstein
R T Zong
D Lin
E J Neufeld
R H Scheuermann
P W Tucker
The University of Texas at Austin · USThe University of Texas Southwestern Medical Center · USDana-Farber Cancer Institute · US

Funding

MAR MEDIATED GENETIC SWITCH FOR IGH ENHANCER CONTROLR01CA031534 · NCI · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI TUCKER, HALEY O · 1985 to 2012
$2.9M
CELL-TYPE SPECIFIC SUPPRESSION OF THE IGH ENHANCERR01GM050329 · NIGMS · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI SCHEUERMANN, RICHARD H · 1996 to 1999
–
REPRESSOR FUNCTION IN MYELOID GENE EXPRESSIONR29HL049196 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI NEUFELD, ELLIS J · 1993 to 1997
–
CELL TYPE SPECIFIC SUPPRESSION OF THE IGH ENHANCERR55GM050329 · NIGMS · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI SCHEUERMANN, RICHARD H · 1994 to 1994
–
NCI NIH HHS CA31534NCI NIH HHS R01 CA031534NHLBI NIH HHS HL49196NIGMS NIH HHS GM50329
6 · The paper itself

Abstract

Nuclear matrix attachment regions (MARs) flanking the immunoglobulin heavy chain intronic enhancer (Emu) are the targets of the negative regulator, NF-muNR, found in non-B and early pre-B cells. Expression library screening with NF-muNR binding sites yielded a cDNA clone encoding an alternatively spliced form of the Cux/CDP homeodomain protein. Cux/CDP fulfills criteria required for NF-muNR identity. It is expressed in non-B and early pre-B cells but not mature B cells. It binds to NF-muNR binding sites within Emu with appropriate differential affinities. Antiserum specific for Cux/CDP recognizes a polypeptide of the predicted size in affinity-purified NF-muNR preparations and binds NF-muNR complexed with DNA. Cotransfection with Cux/CDP represses the activity of Emu via the MAR sequences in both B and non-B cells. Cux/CDP antagonizes the effects of the Bright transcription activator at both the DNA binding and functional levels. We propose that Cux/CDP regulates cell-type-restricted, differentiation stage-specific Emu enhancer activity by interfering with the function of nuclear matrix-bound transcription activators.

Indexed as

Enhancer Elements, GeneticIntronsOncogenesAnimalsBase SequenceBinding SitesCell DifferentiationCell LineCell Line, TransformedDNA-Binding ProteinsDNA, ComplementaryGene Expression RegulationGuinea PigsHomeodomain ProteinsHumansImmunoglobulin mu-ChainsARID3A protein, humanArid3a protein, mouseCUX1 protein, humanCux1 protein, mouseDNA-Binding ProteinsDNA, ComplementaryHomeodomain ProteinsImmunoglobulin mu-ChainsNuclear ProteinsRepressor ProteinsTrans-ActivatorsTranscription Factors

Identifiers

PMID9858552
PMCPMC83886
OpenAlexW2132033022

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.